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1 reatment with a GlyT1 inhibitor or any other investigational drug.
2 ntral fat accumulation were recorded for the investigational drug.
3 act as suitable carriers for the delivery of investigational drugs.
4 o as to improve the efficacy of approved and investigational drugs.
5 creasing prevalence of allosteric ligands as investigational drugs.
6  cell invasive potential form a new class of investigational drugs.
7 s new "breakthrough therapy" designation for investigational drugs adds to the agency's portfolio of
8 d and Drug Administration (FDA)-approved and investigational drugs against hundreds of targets, defin
9 d compare the various therapeutic platforms, investigational drugs, and clinical trials targeting geo
10 l of these proteins have been the targets of investigational drugs, and epidermal growth factor recep
11  leading drug candidates, several designated investigational drugs, and some medical devices, as well
12 ng to abandonment of potentially efficacious investigational drugs, and unexpected deadly adverse eve
13                               Currently only investigational drugs are available in case of radiologi
14 his challenge by testing 128 FDA-approved or investigational drugs as either single agents or in 768
15  research on adherence to placebo-controlled investigational drug by way of drug detection in active-
16 ne-3-carboxamide (VX-770, 48, ivacaftor), an investigational drug candidate approved by the FDA for t
17 asma concentration-time results of NVP-1, an investigational drug candidate, observed in the plasma s
18 F-FDG PET for guiding the selection of novel investigational drugs, choosing dose in early-phase clin
19                               Eritoran is an investigational drug for sepsis treatment that resembles
20 atory scrutiny that affects manufacturers of investigational drugs for early-phase clinical trials en
21       For the past several years a number of investigational drugs have demonstrated activity in pati
22 increases greater than those seen with other investigational drugs in this class and LDL-C lowering e
23                    The mechanistically novel investigational drug ITI-007 was effective for the treat
24 ating agents (HMAs), lenalidomide (LEN), and investigational drugs, may be used after ESA failure in
25             Symptom reduction was 40.7% with investigational drugs (n = 4,510), 41.7% with active com
26                                          The investigational drug, nivolumab, was administered intrav
27 ifies an apoptotic biomarker (PYCARD) for an investigational drug obatoclax.
28  are randomized to standard therapy plus the investigational drug or standard therapy plus placebo ar
29 his method is constrained by the need for an investigational drug permit.
30                                     For both investigational drugs, PET responses tended to be greate
31 d in a 3:1:1 ratio to receive fixed doses of investigational drug, placebo, or haloperidol for 6 week
32           Since the introduction of this new investigational drug, scintigraphic imaging has been per
33 ngs show that transient exposure to this new investigational drug should be useful for controlling p5
34  Task Force of the National Cancer Institute Investigational Drug Steering Committee convened an inte
35 ly reproducible and allows for evaluation of investigational drugs targeting IL-6-dependent MM cells
36  biology of WM and allows the study of novel investigational drugs targeting WM cells in the huBM mil
37 an hepatitis C immune globulin Civacir is an investigational drug that is currently being developed i
38 atitis C immunoglobulin (HCIG) Civacir is an investigational drug that is currently being developed i
39 r (VEGF) therapy and ionizing radiation, and investigational drugs that address different targets alo
40 ents, has led to the clinical development of investigational drugs that restore function to defective
41 reatment of systemic mastocytosis, including investigational drug therapy.
42 nd some of the limitations of this important investigational drug, these findings clearly demonstrate
43 brain tumors referred to our institution for investigational drug trials.
44            It was demonstrated that, for the investigational drug under study, the matrix effect was
45 ity defect can be partially corrected by the investigational drug VX-809 (3-[6-[[[1-(2,2-difluoro-1,3
46 at several of these compounds, including the investigational drug VX-809, caused a much greater incre
47 ue and displayed an additive effect with the investigational drug VX-809.
48                                         This investigational drug was compared with the common antihy
49                                          All investigational drugs were well tolerated.
50 the basis of these data, multiarm studies of investigational drugs will require 25 evaluable subjects

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